Our mission is to improve the health prospects of women living with
lymphangioleio​myomatosis (LAM).

LAM Australia Research Alliance is a not-for-profit organisation run wholly by volunteers.

ABOUT US

  • Funding research to find a cure for LAM
  • Raising awareness of LAM
  • Supporting women living with LAM

DOCTORS WITH LAM EXPERTISE

NEWS

Inaugural Rare Disease Summit, Melbourne, 27-28 March 2015, presented by Rare Voices Australia.  Ros Pollard is representing LAM Australia at the summit. Register ›

The LAM Foundation’s LAMposium will take place in Chicago USA from 26-29 March 2015. More information ›

RESEARCH GIVES HOPE TO WOMEN WITH LAM